Purchase and subsequent delivery of medicinal products: preparations for parenteral nutrition Purchase and subsequent delivery of a medicinal product - TRACE ELEMENTS AND VITAMINS FOR PARENTAL NUTRITION (10)

Purchase and subsequent delivery of medicinal products: preparations for parenteral nutrition Purchase and subsequent delivery of a medicinal product - TRACE ELEMENTS AND VITAMINS FOR PARENTAL NUTRITION (10)
The quality requirements of medicinal products are specified in the Act of September 6, 2001 - Pharmaceutical Law (consolidated text: Journal of Laws of 2016, item 2142, as amended), which in Art. 1(1)(1) states that it specifies, among others: the rules and procedure for authorizing medicinal products to be placed on the market, taking into account in particular the requirements regarding the quality, effectiveness and safety of their use. In addition, the regulation of the Minister of Health of November 9, 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2015, item 1979) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality standard of medicinal products was defined by the Ordering Party by including in the description of the subject of the order, which includes, among others: composition, form and route of administration and unit of measurement